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Variant ID | 71 |
---|---|
Genomic Coordinate (GRCh38) | g.22047062T>G |
Variant | c.200T>G |
Variant Start Position | 200 |
Location | Exon 3 |
Amino Acid Change | p.Leu67* |
ACMG Call | - |
ACMG Call Last Revised Date | 4/28/2021 |
Predicted ACMG Call | Pathogenic | Effect Type | Nonsense |
Variant Type | SNV |
PMID | 16636593, 34806794 |
Article Count | 2 |
Times Observed | < 3 |
Clinical Phenotype | - |
ACMG Categories | pvs1, pm2 |
ACMG Explanations | pvs1: This is a loss of function variant. pm2: chrX:22065180 ref:T alt:A was not found in gnomAD exomes or genomes. chrX:22065180 ref:T alt:G was not found in gnomAD exomes or genomes. |
Variant in Clinvar | No |
ClinVar Classification | - |
Categories In Literature | - |
No Contrary Evidence Found | Yes |
ExAC Allele Frequency | - |
Thousand Genomes Allel Frequency | - |
Ontology Relations | - |
hg19 Mapping Failed | No |
Literature Alleles | X-22065180-T-G |
GnomAD Alleles | - |
DBNSFP Alleles | X-22065180-T-A X-22065180-T-G |
Other Alleles | X-22065180-TA-AG |
Note | nan |
Warnings | - |